Pentiptycenyl Substituents in Insertion Polymerization with α-Diimine Nickel and Palladium Species
| Autor: | Lei Cui, Hongliang Mu, Yudan Liao, Yixin Zhang, Zhongbao Jian |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
chemistry.chemical_classification
Ethylene 010405 organic chemistry Comonomer Organic Chemistry Polymer 010402 general chemistry Branching (polymer chemistry) 01 natural sciences 0104 chemical sciences Inorganic Chemistry chemistry.chemical_compound Monomer chemistry Polymerization Polymer chemistry Copolymer Physical and Theoretical Chemistry Diimine |
| Zdroj: | Organometallics. 38:2075-2083 |
| ISSN: | 1520-6041 0276-7333 |
| DOI: | 10.1021/acs.organomet.9b00106 |
| Popis: | Motivated by the need for a new generation of α-diimine Ni(II) and Pd(II) catalysts for tuning the catalytic activity, polymer molecular weight, comonomer incorporation, and branching density in ethylene polymerization and copolymerization with polar monomers, a family of α-diimine Ni(II) and Pd(II) catalysts Ipty-Ni1–4 and Ipty-Pd1–4 derived from sterically demanding and rotationally restricted pentiptycenyl N-aryl substituents were synthesized and fully characterized by NMR, IR, MALDI-TOF, elemental analysis, and X-ray diffraction. Pentiptycenyl-substituted Ni(II) and Pd(II) catalysts were further probed in ethylene (co)polymerization as a comparison with the rotationally free dibenzhydryl substituent reported previously. In the Ni-catalyzed ethylene polymerization (20–80 °C), catalytic activities ((0.64–3.74) × 106 g mol–1 h–1), polymer molecular weights ((1.1–37.7) × 104 g mol–1), branching densities (6–55/1000C), and melting points (94–135 °C) could be tuned over a broad range. In the Pd-catalyzed et... |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|